FDA 510(k)

LIQUICHEK OPIATE CONTROL

K-Number: K093577 · 2010-03-12

Decision Date2010-03-12

Product CodeDIF

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

LIQUICHEK OPIATE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories. It received FDA 510(k) clearance on 2010-03-12 under 510(k) number K093577. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK OPIATE CONTROL?

LIQUICHEK OPIATE CONTROL is a medical device that received FDA 510(k) clearance on 2010-03-12. The listed applicant is Bio-Rad Laboratories. The 510(k) number is K093577.

When did LIQUICHEK OPIATE CONTROL receive FDA 510(k) clearance?

LIQUICHEK OPIATE CONTROL received FDA 510(k) clearance on 2010-03-12, under 510(k) number K093577.

Who is the listed applicant for LIQUICHEK OPIATE CONTROL?

The FDA 510(k) record lists Bio-Rad Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUICHEK OPIATE CONTROL?

The FDA product code for LIQUICHEK OPIATE CONTROL is DIF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.